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Substances that are too large to directly pass through the cell membrane and do not require ATP for entry typically utilize facilitated diffusion. This process involves specific transport proteins, such as channel or carrier proteins, that help move these substances across the membrane along their concentration gradient. Examples include glucose and ions, which rely on these proteins to enter cells efficiently without energy expenditure.

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What would happen to the size of cell membrane if the a cell were undergo endocytosis and no exocytosis?

If a cell underwent endocytosis without any exocytosis, the size of the cell membrane would gradually decrease as portions of the membrane are internalized to form vesicles. Over time, this could lead to an increase in the cell's internal volume at the expense of the membrane surface area. Eventually, the cell could face issues related to membrane integrity and functionality due to the imbalance between endocytosis and exocytosis.


What is it called when molecules uses energy to move across a semipermeable membrane?

Active transport


What is the difference between facilitated diffusion with the help of a carrier protein and active transport with the help of the transport protein?

Facilitated diffusion is a type of passive transport in which a substance moves across the cell membrane from high to low concentration. In this situation, the substance moves with the concentration gradient, and with the help of carrier molecules, it is able to make it's way across the membrane smoothly and without the expense of energy. Active transport, on the other hand, is the movement of a substance across the cell membrane from low to high concentration, making the transport a bit more difficult and calling for the use of energy. Transport proteins recognize the substance and allow it to cross through the membrane.


Is paying for transportation a fixed expense?

yes


What if cells were in mitosis more than they were in interphase?

If cells were in mitosis more than in interphase, it would lead to rapid cell division at the expense of essential cellular processes such as growth, DNA replication, and repair. This could result in inadequate preparation for division, causing genomic instability and increased risk of mutations. Ultimately, this could disrupt tissue function and contribute to diseases like cancer, as cells would not have enough time to properly carry out their regular functions or maintain cellular integrity.

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